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Lariam (MEFLOQUINE)
Lariam (Mefloquine) is a small molecule antimalarial drug developed by the US Army and currently owned by Roche. It targets the adenosine receptor A2a and is FDA-approved for treating and preventing chloroquine-resistant Plasmodium falciparum malaria, as well as vivax malaria. Lariam is available as a generic medication due to its off-patent status. Key safety considerations include potential neuropsychiatric side effects. It has a high bioavailability of 80%.
At a glance
| Generic name | MEFLOQUINE |
|---|---|
| Sponsor | Roche |
| Drug class | Antimalarial |
| Target | Adenosine receptor A2a |
| Modality | Small molecule |
| Therapeutic area | Metabolic |
| Phase | FDA-approved |
| First approval | 1989 |
Approved indications
- Chloroquine Resistant Plasmodium Falciparum Malaria
- Chloroquine-Resistant Plasmodium Falciparum Malaria Prevention
- Vivax malaria
Boxed warnings
- WARNING Mefloquine may cause neuropsychiatric adverse reactions that can persist after mefloquine has been discontinued. Mefloquine should not be prescribed for prophylaxis in patients with major psychiatric disorders. During prophylactic use, if psychiatric or neurologic symptoms occur, the drug should be discontinued and an alternative medication should be substituted (see WARNINGS ).
Common side effects
- Vomiting
- Dizziness
- Nausea
- Diarrhea
- Headache
- Fever
- Chills
- Abdominal pain
- Fatigue
- Loss of appetite
- Tinnitus
- Myalgia
Drug interactions
- P-glycoprotein Substrates
- halofantrine
- rifampicin
- ziprasidone
Key clinical trials
- A Trial to Compare the Efficacy, Safety and Tolerability of Combinations of 3 Anti-malarial Drugs Against Combina-tions of 2 Anti-malarial Drugs. (PHASE3)
- FocaL Mass Drug Administration for Vivax Malaria Elimination (PHASE3)
- Temozolomide, Memantine Hydrochloride, Mefloquine, and Metformin Hydrochloride in Treating Patients With Glioblastoma Multiforme After Radiation Therapy (PHASE1)
- A Trial to Compare the Efficacy, Safety and Tolerability of Combinations of 3 Anti-malarial Drugs Against Combinations of 2 Anti-malarial Drugs (Asia) (PHASE3)
- Safety and Efficacy of NF135 CPS Immunization (NA)
- Efficacy of Mefloquine as Prophylaxis Against COVID-19: A Placebo-control, Randomized Clinical Trial (PHASE2,PHASE3)
- Study of Efficacy and Safety of TL-FVP-t vs. SOC in Patients With Mild to Moderate COVID-19 (PHASE3)
- Compare the Effectiveness Between Existing Treatment and New Treatment (NA)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| FDA label | Mechanism, indications, dosing, boxed warnings, drug interactions |
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |